Department of Integrative Neurophysiology, Center for Neurogenomics and Cognitive Research, Neuroscience Campus Amsterdam, VU University Amsterdam, Room C-440, De Boelelaan 1085, 1081 HV Amsterdam, The Netherlands.
Neural Plast. 2011;2011:870763. doi: 10.1155/2011/870763. Epub 2011 Sep 15.
Throughout life, activity-dependent changes in neuronal connection strength enable the brain to refine neural circuits and learn based on experience. In line with predictions made by Hebb, synapse strength can be modified depending on the millisecond timing of action potential firing (STDP). The sign of synaptic plasticity depends on the spike order of presynaptic and postsynaptic neurons. Ionotropic neurotransmitter receptors, such as NMDA receptors and nicotinic acetylcholine receptors, are intimately involved in setting the rules for synaptic strengthening and weakening. In addition, timing rules for STDP within synapses are not fixed. They can be altered by activation of ionotropic receptors located at, or close to, synapses. Here, we will highlight studies that uncovered how network actions control and modulate timing rules for STDP by activating presynaptic ionotropic receptors. Furthermore, we will discuss how interaction between different types of ionotropic receptors may create "timing" windows during which particular timing rules lead to synaptic changes.
在整个生命过程中,神经元连接强度的活动依赖性变化使大脑能够根据经验精细调整神经回路和学习。符合赫布的预测,突触强度可以根据动作电位发射的毫秒定时(STDP)进行修改。突触可塑性的符号取决于突触前和突触后神经元的尖峰顺序。离子型神经递质受体,如 NMDA 受体和烟碱型乙酰胆碱受体,密切参与设定突触增强和减弱的规则。此外,突触内 STDP 的定时规则不是固定的。它们可以通过激活位于突触或靠近突触的离子型受体来改变。在这里,我们将重点介绍阐明网络活动如何通过激活突触前离子型受体来控制和调节 STDP 的定时规则的研究。此外,我们将讨论不同类型的离子型受体之间的相互作用如何在特定的定时规则导致突触变化的“定时”窗口期间产生。